C4540497[trait identifier] AND "Equipe Genetique des Anomalies du Deve - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2445216	NM_001142966.3(GREB1L):c.833A>T (p.Asp278Val)	GREB1L, LOC101927521 (D278V +1 more)	Single nucleotide variant (missense variant)	Renal hypodysplasia/aplasia 3	GUncertain significance
Select item 1172634	NM_001142966.3(GREB1L):c.2252G>A (p.Arg751His)	GREB1L (R751H)	Single nucleotide variant (missense variant)	Renal hypodysplasia/aplasia 3 +1 more	GLikely pathogenic